Chitanava Tamara, Matvienko Iuliia, Shuvaev Vasily, Voloshin Sergey, Martynkevich Irina, Vlasova Yulia, Efremova Elizaveta, Mileeva Ekaterina, Pirkhalo Anna, Makarova Taiana, Vlasik Roman, Karyagina Elena, Il Ina Natalia, Medvedeva Nadezhda, Dorofeeva Natalia, Shneider Tatiana, Siordiya Nadia, Kulemina Olga, Sbityakova Evgenia, Lazorko Natalia, Alexeeva Julia, Motorin Dmitrii, Morozova Elena, Lomaia Elza
Research Department of Immuno-Oncology, Almazov National Medical Research Centre, Saint Petersburg, Russia.
Clinical and Diagnostic Department of Hematology and Chemotherapy with a Day Patient Facility, Russian Research Institute of Hematology and Transfusiology, Saint Petersburg, Russia.
Front Oncol. 2023 Mar 16;13:1138683. doi: 10.3389/fonc.2023.1138683. eCollection 2023.
Tyrosine kinase inhibitor (TKI) therapy has greatly improved the prognosis of patients with chronic myeloid leukemia (CML), improving the survival expectancy of patients with chronic phase (CP) CML to that of the general population. However, despite these advances, nearly 50% of patients with CP CML experience failure to respond to frontline therapy, and most fail to respond to the subsequent second-line TKI. Treatment guidelines for patients failing second-line therapy are lacking. This study aimed to determine the efficacy of TKIs as third-line therapy in a "real-world" clinical practice setting and identify factors favorably influencing the long-term outcomes of therapy.
We have retrospectively analyzed the medical records of 100 patients with CP CML.
The median age of the patients was 51 (range, 21-88) years, and 36% of the patients were men. The median duration of the third-line TKI therapy was 22 (range, 1- 147) months. Overall, the rate of achieving complete cytogenetic response (CCyR) was 35%. Among the four patient groups with different levels of responses at baseline, the best results were achieved in the groups with any CyR at the baseline of third-line therapy. Thus, СCyR was reached in all 15 and 8/ 16 (50%) patients with partial cytogenetic response (PCyR) or minimal or minor CyR (mmCyR), respectively, whereas CCyR was detected only in 12/69 (17%) patients without any CyR at baseline (p < 0.001). Univariate regression analysis revealed that the factors negatively associated with CCyR achievement in thirdline TKI therapy were the absence of any CyR on first- or second-line TKI therapy (p < 0.001), absence of CHR prior to third-line TKI (p = 0.003), and absence of any CyR prior to third-line TKI (p < 0.001). During the median observation time from treatment initiation to the last visit [56 (4-180) months], 27% of cases progressed into accelerated phase or blast phase CML, and 32% of patients died.
Progression-free survival (PFS) and overall survival (OS) were significantly higher in patients with CCyR on third-line than in the group without CCyR on third-line therapy. At the last visit, third-line TKI therapy was ongoing in 18% of patients, with a median time of treatment exposure of 58 (range, 6-140) months; 83% of these patients had stable and durable CCyR, suggesting that patients without CHR at baseline and without CCyR at least by 12 months on third-line TKI should be candidates for allogeneic stem cell transplantation, third-generation TKIs, or experimental therapies.
酪氨酸激酶抑制剂(TKI)疗法极大地改善了慢性髓性白血病(CML)患者的预后,将慢性期(CP)CML患者的预期生存期提高到了普通人群的水平。然而,尽管有这些进展,近50%的CP CML患者一线治疗无效,且大多数患者对后续二线TKI治疗也无反应。目前缺乏针对二线治疗失败患者的治疗指南。本研究旨在确定TKI作为三线治疗在“真实世界”临床实践中的疗效,并确定对治疗长期结果有积极影响的因素。
我们回顾性分析了100例CP CML患者的病历。
患者的中位年龄为51岁(范围21 - 88岁),36%为男性。三线TKI治疗的中位持续时间为22个月(范围1 - 147个月)。总体而言,完全细胞遗传学缓解(CCyR)率为35%。在基线时有不同反应水平的四组患者中,三线治疗基线时有任何细胞遗传学缓解(CyR)的组取得了最佳结果。因此,分别有15例部分细胞遗传学缓解(PCyR)患者和所有8/16例(50%)微小或轻度CyR(mmCyR)患者达到了CCyR,而基线时无任何CyR的69例患者中仅有12/69例(17%)检测到CCyR(p < 0.001)。单因素回归分析显示,与三线TKI治疗中实现CCyR呈负相关的因素为一线或二线TKI治疗时无任何CyR(p < 0.001)、三线TKI治疗前无细胞遗传学缓解(CHR)(p = 0.003)以及三线TKI治疗前无任何CyR(p < 0.001)。在从治疗开始到最后一次随访的中位观察时间[56(4 - 180)个月]内,27%的病例进展为加速期或急变期CML,32%的患者死亡。
三线治疗达到CCyR的患者的无进展生存期(PFS)和总生存期(OS)显著高于三线治疗未达到CCyR的组。在最后一次随访时,1 / 8的患者正在接受三线TKI治疗,治疗暴露的中位时间为58个月(范围6 - 140个月);这些患者中有83%具有稳定且持久的CCyR,这表明基线时无CHR且三线TKI治疗至少12个月未达到CCyR的患者应考虑进行异基因干细胞移植、第三代TKI或实验性治疗。